FDA Inspection 849797 — Kevin Waltz, OD, MD

Kevin Waltz, OD, MD — FEI 3009453953

The FDA completed an inspection of Kevin Waltz, OD, MD on Sep 20, 2013 in Indianapolis, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 20, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Indianapolis, IN (United States)

Additional Details

Clinical Investigator (CI)